6-Benzyloxymethyl-4-hydroxypyrimidine is a chemical compound characterized by its pyrimidine core, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a hydroxyl group (-OH) at the 4-position contributes to its potential as a biological active molecule, possibly influencing its solubility and reactivity. The benzyloxymethyl group at the 6-position enhances the compound's lipophilicity, which may improve its ability to penetrate biological membranes. This compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry. Its structure suggests potential applications in drug development, particularly in targeting specific biological pathways. The CAS number 188177-37-9 uniquely identifies this substance, facilitating its recognition in chemical databases and literature. As with many organic compounds, its stability, reactivity, and interactions with other molecules can be influenced by environmental conditions such as pH and temperature. Further studies would be necessary to fully elucidate its properties and potential applications in various fields, including pharmaceuticals and biochemistry.

6-BENZYLOXYMETHYL-4-HYDROXYPYRIMIDINE

188177-37-9: 6-Benzyloxymethyl-4-hydroxypyrimidine is a chemical compound characterized by its pyrimidine core, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a hydroxyl group (-OH) at the 4-position contributes to its potential as a biological active molecule, possibly influencing its solubility and reactivity. The benzyloxymethyl group at the 6-position enhances the compound's lipophilicity, which may improve its ability to penetrate biological membranes. This compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry. Its structure suggests potential applications in drug development, particularly in targeting specific biological pathways. The CAS number 188177-37-9 uniquely identifies this substance, facilitating its recognition in chemical databases and literature. As with many organic compounds, its stability, reactivity, and interactions with other molecules can be influenced by environmental conditions such as pH and temperature. Further studies would be necessary to fully elucidate its properties and potential applications in various fields, including pharmaceuticals and biochemistry.

CAS 188177-37-9

6-BENZYLOXYMETHYL-4-HYDROXYPYRIMIDINE

6-Benzyloxymethyl-4-hydroxypyrimidine

Ref: IN-DA002GQO